# Dantec Electronics, Inc.

- Location (FDA's records): Allendale, NJ
- FDA decisions: 12 (1985–1990): 12 510(k) clearances
- Product codes: GWF (4), FAP (3), FFO (2), GXY (1), GXZ (1), IKT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Rochester Electro Medical, Inc.: 1 (https://510kreport.com/company/rochester-electro-medical)
- Neurovision Medical Products, Inc.: 1 (https://510kreport.com/company/neurovision-medical-products)

## Its most-cited devices
- K895460: Concentric Electrode Type #13R01, 13R02 (1990), cited by 1
- K874758: Dantec 13L40 ST. Marks's Pudendal Electrode (1988), cited by 1

## Recent decisions
- K895460: Concentric Electrode Type #13R01, 13R02 (Jun 18, 1990)
- K894911: Sensory Needle Electrode Dne 111-115,116-117,118 (May 14, 1990)
- K884915: Dantec 22K60/61/62 Catheter Tip Transducer (Oct 4, 1989)
- K881915: Dantec Magnetic Stimulator (Oct 17, 1988)
- K874759: 13L81 Disposable Sphincter Electrode, 13L33 Cable (Apr 14, 1988)
- K874758: Dantec 13L40 ST. Marks's Pudendal Electrode (Apr 14, 1988)
- K874735: Dantec 13L35/36/37 Stim. and Recording Electrode (Jan 22, 1988)
- K870567: Evoport 300 (Oct 6, 1987)

Source page: https://510kreport.com/company/dantec-electronics